Canonical Allele Identifier: CA2669711121

Gene: MSANTD1

Linked Data

• gnomAD v4: 4-3256487-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3256487T>G , CM000666.2:g.3256487T>G	GRCh38
NC_000004.11:g.3258214T>G , CM000666.1:g.3258214T>G	GRCh37
NC_000004.10:g.3228012T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000438480.7:c.*522T>G MANE Select	ENSP00000411584.2:n.*522T>G
ENST00000505599.5:c.729+630T>G	ENSP00000425405.1:n.729+630T>G
ENST00000507492.5:c.*522T>G	ENSP00000423547.1:n.*522T>G
ENST00000510580.1:c.765+594T>G	ENSP00000420966.1:n.765+594T>G
NM_001042690.1:c.*522T>G	NP_001036155.1:n.*522T>G
XM_006713883.2:c.*522T>G	XP_006713946.1:n.*522T>G
XM_011513464.1:c.729+630T>G	XP_011511766.1:n.729+630T>G
XM_011513465.1:c.*522T>G	XP_011511767.1:n.*522T>G
XM_011513466.1:c.*522T>G	XP_011511768.1:n.*522T>G
XM_011513467.1:c.*522T>G	XP_011511769.1:n.*522T>G
XR_924950.1:n.753+630T>G
NM_001330620.1:c.*522T>G	NP_001317549.1:n.*522T>G
XM_011513466.3:c.*522T>G	XP_011511768.1:n.*522T>G
XM_011513467.3:c.*522T>G	XP_011511769.1:n.*522T>G
NM_001042690.2:c.*522T>G MANE Select	NP_001036155.1:n.*522T>G
NM_001330620.2:c.*522T>G	NP_001317549.1:n.*522T>G